| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5222990 | Tetrahedron | 2009 | 7 Pages |
Abstract
In this work, we describe the synthesis of new 2,4,5-trisubstituted-1,3-thiazoles and 1,3-selenazole achieved by an easy one-pot four-step procedure. Expected compounds were obtained in good yield from dimethyl cyanodithioimidocarbonate, which was the common starting material for the preparation of all 1,3-thiazoles and 1,3-selenazoles. Chemical diversity was introduced on thiazole and selenazole rings by varying the amines and the activated halides used.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
David Thomae, Enrico Perspicace, Zhanjie Xu, Dorothée Henryon, Serge Schneider, Stéphanie Hesse, Gilbert Kirsch, Pierre Seck,